GSM4105305: COG-N-415 H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq

SRX6937021 GSM4105305 GSM4105305: COG-N-415 H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467033 GSM4105305 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105305 GSM4105305 GEO Accession GSM4105305 SRX6937022 GSM4105306 GSM4105306: COG-N-415 H3K4me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467034 GSM4105306 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105306 GSM4105306 GEO Accession GSM4105306 SRX6937023 GSM4105307 GSM4105307: COG-N-415 Input histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467035 GSM4105307 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105307 GSM4105307 GEO Accession GSM4105307 SRX6937024 GSM4105308 GSM4105308: KELLY H3K27Ac histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467036 GSM4105308 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105308 GSM4105308 GEO Accession GSM4105308 SRX6937025 GSM4105309 GSM4105309: KELLY H3K27me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467037 GSM4105309 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105309 GSM4105309 GEO Accession GSM4105309 SRX6937026 GSM4105310 GSM4105310: KELLY H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467038 GSM4105310 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105310 GSM4105310 GEO Accession GSM4105310 SRX6937027 GSM4105311 GSM4105311: KELLY H3K4me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467039 GSM4105311 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105311 GSM4105311 GEO Accession GSM4105311 SRX6937028 GSM4105312 GSM4105312: KELLY Input histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467040 GSM4105312 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105312 GSM4105312 GEO Accession GSM4105312 SRX6937029 GSM4105313 GSM4105313: LA-N-5 H3K27Ac histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467041 GSM4105313 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105313 GSM4105313 GEO Accession GSM4105313 SRX6937030 GSM4105314 GSM4105314: LA-N-5 H3K27me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467042 GSM4105314 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105314 GSM4105314 GEO Accession GSM4105314 SRX6937031 GSM4105315 GSM4105315: LA-N-5 H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467043 GSM4105315 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105315 GSM4105315 GEO Accession GSM4105315 SRX6937032 GSM4105316 GSM4105316: LA-N-5 H3K4me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467044 GSM4105316 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105316 GSM4105316 GEO Accession GSM4105316 SRX6937033 GSM4105317 GSM4105317: LA-N-5 Input histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467045 GSM4105317 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105317 GSM4105317 GEO Accession GSM4105317 SRX6937034 GSM4105318 GSM4105318: NB-1643 H3K27Ac histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467046 GSM4105318 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105318 GSM4105318 GEO Accession GSM4105318 SRX6937035 GSM4105319 GSM4105319: NB-1643 H3K27me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467047 GSM4105319 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105319 GSM4105319 GEO Accession GSM4105319 SRX6937036 GSM4105320 GSM4105320: NB-1643 H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467048 GSM4105320 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105320 GSM4105320 GEO Accession GSM4105320 SRX6937037 GSM4105321 GSM4105321: NB-1643 H3K4me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467049 GSM4105321 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105321 GSM4105321 GEO Accession GSM4105321 SRX6937038 GSM4105322 GSM4105322: NB-1643 Input histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467050 GSM4105322 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105322 GSM4105322 GEO Accession GSM4105322 SRX6937039 GSM4105323 GSM4105323: NB-69 H3K27Ac histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467051 GSM4105323 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105323 GSM4105323 GEO Accession GSM4105323 SRX6937040 GSM4105324 GSM4105324: NB-69 H3K27me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467052 GSM4105324 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105324 GSM4105324 GEO Accession GSM4105324 SRX6937041 GSM4105325 GSM4105325: NB-69 H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467053 GSM4105325 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105325 GSM4105325 GEO Accession GSM4105325 SRX6937042 GSM4105326 GSM4105326: NB-69 H3K4me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467054 GSM4105326 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105326 GSM4105326 GEO Accession GSM4105326 SRX6937043 GSM4105327 GSM4105327: NB-69 Input histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467055 GSM4105327 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105327 GSM4105327 GEO Accession GSM4105327 SRX6937044 GSM4105328 GSM4105328: NBL-S H3K27Ac histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467056 GSM4105328 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105328 GSM4105328 GEO Accession GSM4105328 SRX6937045 GSM4105329 GSM4105329: NBL-S H3K27me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467057 GSM4105329 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105329 GSM4105329 GEO Accession GSM4105329 SRX6937046 GSM4105330 GSM4105330: NBL-S H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467058 GSM4105330 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105330 GSM4105330 GEO Accession GSM4105330 SRX6937047 GSM4105331 GSM4105331: NBL-S H3K4me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467059 GSM4105331 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105331 GSM4105331 GEO Accession GSM4105331 SRX6937048 GSM4105332 GSM4105332: NBL-S Input histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467060 GSM4105332 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105332 GSM4105332 GEO Accession GSM4105332 SRX6937049 GSM4105333 GSM4105333: NGP H3K27Ac histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467061 GSM4105333 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105333 GSM4105333 GEO Accession GSM4105333 SRX6937050 GSM4105334 GSM4105334: NGP H3K27me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467062 GSM4105334 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105334 GSM4105334 GEO Accession GSM4105334 SRX6937051 GSM4105335 GSM4105335: NGP H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467063 GSM4105335 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105335 GSM4105335 GEO Accession GSM4105335 SRX6937052 GSM4105336 GSM4105336: NGP H3K4me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467064 GSM4105336 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105336 GSM4105336 GEO Accession GSM4105336 SRX6937053 GSM4105337 GSM4105337: NGP Input histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467065 GSM4105337 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105337 GSM4105337 GEO Accession GSM4105337 SRX6937054 GSM4105338 GSM4105338: SK-N-AS H3K27Ac histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467066 GSM4105338 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105338 GSM4105338 GEO Accession GSM4105338 SRX6937055 GSM4105339 GSM4105339: SK-N-AS H3K27me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467067 GSM4105339 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105339 GSM4105339 GEO Accession GSM4105339 SRX6937056 GSM4105340 GSM4105340: SK-N-AS H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467068 GSM4105340 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105340 GSM4105340 GEO Accession GSM4105340 SRX6937057 GSM4105341 GSM4105341: SK-N-AS H3K4me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467069 GSM4105341 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105341 GSM4105341 GEO Accession GSM4105341 SRX6937058 GSM4105342 GSM4105342: SK-N-AS Input histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467070 GSM4105342 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105342 GSM4105342 GEO Accession GSM4105342 SRX6937059 GSM4105343 GSM4105343: SK-N-BE(2)-C H3K27Ac histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467071 GSM4105343 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105343 GSM4105343 GEO Accession GSM4105343 SRX6937060 GSM4105344 GSM4105344: SK-N-BE(2)-C H3K27me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467072 GSM4105344 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105344 GSM4105344 GEO Accession GSM4105344 SRX6937061 GSM4105345 GSM4105345: SK-N-BE(2)-C H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467073 GSM4105345 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105345 GSM4105345 GEO Accession GSM4105345 SRX6937062 GSM4105346 GSM4105346: SK-N-BE(2)-C H3K4me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467074 GSM4105346 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105346 GSM4105346 GEO Accession GSM4105346 SRX6937063 GSM4105347 GSM4105347: SK-N-BE(2)-C Input histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467075 GSM4105347 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105347 GSM4105347 GEO Accession GSM4105347 SRX6937064 GSM4105348 GSM4105348: SK-N-FI H3K27Ac histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467076 GSM4105348 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105348 GSM4105348 GEO Accession GSM4105348 SRX6937065 GSM4105349 GSM4105349: SK-N-FI H3K27me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467077 GSM4105349 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105349 GSM4105349 GEO Accession GSM4105349 SRX6937066 GSM4105350 GSM4105350: SK-N-FI H3K4me1 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467078 GSM4105350 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105350 GSM4105350 GEO Accession GSM4105350 SRX6937067 GSM4105351 GSM4105351: SK-N-FI H3K4me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467079 GSM4105351 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105351 GSM4105351 GEO Accession GSM4105351 SRX6937068 GSM4105352 GSM4105352: SK-N-FI Input histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467080 GSM4105352 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105352 GSM4105352 GEO Accession GSM4105352 SRX6937069 GSM4105303 GSM4105303: COG-N-415 H3K27Ac histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467081 GSM4105303 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105303 GSM4105303 GEO Accession GSM4105303 SRX6937070 GSM4105304 GSM4105304: COG-N-415 H3K27me3 histone-ChIP-Seq; Homo sapiens; ChIP-Seq SRP223977 SRS5467082 GSM4105304 ChIP-Seq GENOMIC ChIP For ChIP-Seq, cells were crosslinked, flash frozen, and sent to Active Motif. According to Active Motif protocol, cells were lysed, sonicated, and then DNA-protein complexes were isolated with antibodies. Samples were reverse-crosslinked and DNA was purified. For ATAC-Seq, whole cells were frozen and sent to Active Motif for thawing and transposition. Illumina libraries were prepared by Active Motif using standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After 15 cycles of PCR amplification, the resulting DNA libraries were quantified and sequenced by Jefferson Cancer Genomics Laboratory at the Kimmel Cancer Center using the NexSeq 500. NextSeq 500 gds 304105304 GSM4105304 GEO Accession GSM4105304